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Q37371636-FFEA3095-7CF8-4688-BFC6-7C5EAB7EE435
Q37371636-FFEA3095-7CF8-4688-BFC6-7C5EAB7EE435
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Statement
http://www.wikidata.org/entity/statement/Q37371636-FFEA3095-7CF8-4688-BFC6-7C5EAB7EE435
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
P2860
Q37371636-FFEA3095-7CF8-4688-BFC6-7C5EAB7EE435
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37371636-FFEA3095-7CF8-4688-BFC6-7C5EAB7EE435
rank
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wasDerivedFrom
8c0ed825f8aa3cb0dbafacec56c9a9b3c61627b4
P2860
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia